Losartan Potassium
- Product NDC
- 60429-863
- 11-digit product format
- 604290863
- Labeler code
- 60429
- Product ID
- 60429-863_9bbe818e-c816-a2a2-e053-2995a90a41c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA076958
- Marketing category
- ANDA
- Marketing start
- 2010-04-06
- Marketing end
- 2020-02-03
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0d341e63-aee5-498b-bf9a-b53a43963acf | Product name | 1 | 20260105 |
| de29c5c0-90ba-29da-d7ab-0500274708be | Product name | 6 | 20241009 |
| 362d7abb-94e6-4c60-9a58-266894157713 | Product name | 1 | 20231023 |
| 594e2c86-3079-4e6e-96c9-48f7a8afc78d | Product name | 1 | 20230718 |
| 351abe41-466c-4dd8-840a-0fdb68318bd5 | Product name | 1 | 20230316 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 15b375b1-89c7-9594-80df-5a8c8864aee0 | Product name | 3 | 20180108 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
| d723478e-ad4a-ec23-6bd7-cfe33e1e3840 | Product name | 1 | 20140508 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 60429-863-10 | EA - Each | 60429-863 | 890dfe87-8dec-4c4f-8158-cc71d7c4e417 | 1 | 2017-11-06 |
| 60429-863-30 | EA - Each | 60429-863 | 433bfbb2-bf39-45c1-a1e1-d0e6f7ebc06b | 1 | 2017-11-06 |
| 60429-863-90 | EA - Each | 60429-863 | 95e2e8d9-5b79-45f5-8786-a6248356b8cf | 1 | 2017-11-06 |